Filament for three-dimensional modeling, three-dimensional modeled article, three-dimensional modeling method, and three-dimensional modeling apparatus

ABSTRACT

A filament for three-dimensional modeling includes a first resin; a second resin; a fiber; and a compatibilizing agent, wherein a fiber coated with the second resin is dispersed in a matrix formed of the first resin, the compatibilizing agent is interposed between the first resin and the second resin, a thickness of a coating layer formed of the second resin is 0.1 μm or more and 5 μm or less, and a content rate of the second resin with respect to a total weight of the first resin, the second resin, and the compatibilizing agent is 30% by weight or more and 50% by weight or less, or 5% by weight or more and 15% by weight or less.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is based on and claims priority under 35 USC 119 fromJapanese Patent Application No. 2020-056637 filed Mar. 26, 2020.

BACKGROUND (i) Technical Field

The present invention relates to a filament for three-dimensionalmodeling, a three-dimensional modeled article, a three-dimensionalmodeling method, and a three-dimensional modeling apparatus.

(ii) Related Art

Known is a fused deposition modeling (also referred to as FDM)-typemodeling method in which a three-dimensional modeled article is modeledby discharging a plurality of heated filaments onto a discharge targetbody and stacking the filaments to form a laminate.

The filament (hereinafter, also referred to as the filament forthree-dimensional modeling) includes, for example, a resin and a fiber.

Separately from the filament for three-dimensional modeling, an exampleof a composite material including a fiber and a resin is a long carbonfiber-reinforced composite material described in Japanese Patent No.5712464. The long carbon fiber-reinforced composite material includes 30to 250 parts by weight of maleic anhydride-modified polypropylene (B)having a melt flow rate of 30 to 150 g/10 min and 1 to 50 parts byweight of a polyamide resin (C) with respect to 100 parts by weight of a7.5 mm or longer long carbon fiber (A) and includes (B) and (C) in atotal content of 35 to 260 parts by weight.

In addition, Japanese Patent No. 6012914 describes a carbonfiber-reinforced resin composition including 100 parts by weight of apolymer alloy (A) and 1 to 200 parts by weight of a carbon fiber (B),the polymer alloy (A) including 25% to 95% by weight of one or morekinds of propylene-based polymers (p) selected from a propylene-ethyleneblock copolymer, a propylene homopolymer, and a propylene-ethylenerandom copolymer having an ethylene content of 5% by weight or less, 1%to 60% by weight of an acid-modified polyolefin resin (m), 0% to 40% byweight of an ethylene-based polymer (e), and 0% to 50% by weight of apolyamide (n) (here, the total of the component (p), the component (m),the component (e), and the component (n) is 100% by weight).

SUMMARY

As described above, the filament for three-dimensional modelingincludes, for example, a resin and a fiber, and a three-dimensionalmodeled article is obtained by applying the filament forthree-dimensional modeling to a fused deposition modeling-type modelingmethod. However, there is a case where the bending elastic modulus ofthe obtained three-dimensional modeled article is not sufficient and theobtained three-dimensional modeled article absorbs water to causedeterioration.

Therefore, aspects of non-limiting embodiments of the present disclosurerelate to a filament for three-dimensional modeling which provides athree-dimensional modeled article having an excellent bending elasticmodulus as compared with a filament for three-dimensional modeling inwhich a fiber coated with the second resin is dispersed in a matrixformed of the first resin, the compatibilizing agent is interposedbetween the first resin and the second resin, and (1) a thickness of acoating layer formed of the second resin is less than 0.1 μm or morethan 5 μm, or (2) a content rate of the second resin with respect to atotal weight of the first resin, the second resin, and thecompatibilizing agent is less than 5% by weight, more than 15% by weightand less than 30% by weight, or more than 50% by weight.

Aspects of certain non-limiting embodiments of the present disclosureovercome the above disadvantages and/or other disadvantages notdescribed above. However, aspects of the non-limiting embodiments arenot required to overcome the disadvantages described above, and aspectsof the non-limiting embodiments of the present disclosure may notovercome any of the disadvantages described above.

According to an aspect of the present disclosure, there is provided afilament for three-dimensional modeling, including:

a first resin;

a second resin;

a fiber; and

a compatibilizing agent, wherein a fiber coated with the second resin isdispersed in a matrix formed of the first resin,

the compatibilizing agent is interposed between the first resin and thesecond resin,

a thickness of a coating layer formed of the second resin is 0.1 μm ormore and 5 μm or less, and

a content rate of the second resin with respect to a total weight of thefirst resin, the second resin, and the compatibilizing agent is 30% byweight or more and 50% by weight or less, or 5% by weight or more and15% by weight or less.

BRIEF DESCRIPTION OF THE DRAWINGS

Exemplary embodiments of the present invention will be described indetail based on the following FIGURE, wherein:

FIG. 1 shows a schematic view of an example of a three-dimensionalmodeling apparatus according to the exemplary embodiment.

DETAILED DESCRIPTION

Hereinafter, an exemplary embodiment, which is an example of a filamentfor three-dimensional modeling of the present invention, will bedescribed.

<Filament for Three-Dimensional Modeling>

In a filament for three-dimensional modeling according to the exemplaryembodiment (hereinafter, also simply referred to as the “filament”), afiber coated with a second resin is dispersed in a matrix formed of afirst resin, a compatibilizing agent is interposed between the firstresin and the second resin, the thickness of a coating layer formed ofthe second resin is 0.1 μm or more and 5 μm or less, and the contentrate of the second resin with respect to the total weight of the firstresin, the second resin, and the compatibilizing agent is 30% by weightor more and 50% by weight or less, or 5% by weight or more and 15% byweight or less.

According to the filament according to the exemplary embodiment, athree-dimensional modeled article that has an excellent bending elasticmodulus and prevents from absorbing water and causing deterioration canbe obtained. The reason therefor is not clear, but is assumed asdescribed below.

The filament according to the exemplary embodiment has a form in which afiber coated with a second resin is dispersed in a matrix formed of afirst resin, and a compatibilizing agent is interposed between the firstresin and the second resin.

The above-described form shows that the fiber is coated with the secondresin, whereby the second resin is superior to the first resin in termsof adhesion to the fiber. In addition, the compatibilizing agent isinterposed between the first resin and the second resin, and therefore,the adhesion between the first resin, which forms the matrix, and thesecond resin is excellent, as compared with a case where thecompatibilizing agent is not interposed.

Based on the above-described facts, it is considered that, since theadhesion between the fiber and the resin components (here, the firstresin and the second resin) is improved, the mechanical characteristics(specifically, bending elastic modulus) of an obtained three-dimensionalmodeled article is improved.

In addition, from the viewpoint of improving the adhesion to the fiber,it is effective to use resins having a polar group as the resinsincluded in the filament, but there is a problem in that athree-dimensional modeled article including a resin having a polar groupeasily absorbs water due to the polar group.

In the case of the filament according to the exemplary embodiment, it isconsidered that since two kinds of resins, which are the first resin andthe second resin, are used, it is possible to prevent water absorptioneven in the case of, for example, using a resin having a polar group asthe second resin. Specifically speaking, the second resin is present inthe matrix formed of the first resin, coats the fiber, and has a contentrate in the above-described range. Based on this fact, it is assumedthat water absorption by the polar group in the second resin does noteasily develop, thereby making it possible to efficiently prevent athree-dimensional modeled article from absorbing water.

[Preferred Aspect of Filament]

The filament according to the exemplary embodiment is preferably anaspect below.

In the filament according to the exemplary embodiment, the thickness ofthe coating layer formed of the second resin is 0.1 μm or more and 5 μmor less, preferably 0.2 μm or more and 3 μm or less, and more preferably0.5 μm or more and 2 μm or less.

The method for measuring the thickness of the coating layer formed ofthe second resin is as described below.

The thickness of the coating layer formed of the second resin ismeasured by observing the cross section of the filament in a directionorthogonal to the axis.

The filament according to the exemplary embodiment is cut in thedirection orthogonal to the axis to obtain a cross section in thedirection orthogonal to the axis. Subsequently, the cross section ispolished and is coated with osmium using a Neo Osmium Coater (Neoc-PROmanufactured by Meiwafosis Co., Ltd.) to obtain an observation surface.

Next, backscattered electron images of three visual fields on theobservation surface are randomly captured using SEM (S-3400Nmanufactured by Hitachi, Ltd., accelerating voltage of 15 KV) at amagnification of 100 times to 1000 times.

Based on the captured photograph, the thickness of the coating layerformed of the second resin, which is formed on the circumference of thefiber, is obtained using image analysis software (LUZEX by NirecoCorporation).

This procedure is carried out on the photographs of the three capturedvisual fields, and the arithmetic average value of the obtained valuesis regarded as the “thickness of the coating layer formed of the secondresin” in the exemplary embodiment.

In the filament according to the exemplary embodiment, from theviewpoint of obtaining a three-dimensional modeled article that has anexcellent bending elastic modulus and does not easily absorb water, thecoating rate of the fiber with the second resin is preferably 70% ormore, more preferably 80% or more, and still more preferably 90% ormore.

The upper limit of the coating rate of the fiber with the second resinis 100%.

The method for measuring the coating rate of the fiber with the secondresin is as described below.

The coating rate of the fiber with the second resin is measured byobserving the cross section of the filament in the direction orthogonalto the axis.

First, three visual fields on the observation surface are captured usingSEM by the same method as in the measurement of the thickness of thecoating layer formed of the second resin.

Based on the captured photograph, how much of the circumference of thefiber is coated with the second resin is obtained using image analysissoftware (LUZEX by Nireco Corporation).

This procedure is carried out on the photographs of the three capturedvisual fields, and the arithmetic average value of the obtained valuesis regarded as the coating rate of the fiber with the second resin inthe cross section in the direction orthogonal to the axis.

In the filament according to the exemplary embodiment, thecompatibilizing agent is interposed between the first resin and thesecond resin.

That is, the compatibilizing agent is present between the first resin,which forms the matrix, and the second resin, which coats thecircumference of the fiber.

Whether or not the compatibilizing agent is interposed between the firstresin and the second resin is confirmed as described below.

The filament according to the exemplary embodiment is cut in thedirection orthogonal to the axis to obtain a cross section in thedirection orthogonal to the axis. Subsequently, the cross section ispolished, and the filament is buried in an epoxy resin, therebyobtaining a test piece. From this test piece, a thin film test piece isproduced using a microtome (NANOCUT R manufactured by Leica BiosystemsInc.), and whether or not the compatibilizing agent is interposedbetween the first resin and the second resin is observed with STEM/EDX(HF-3300 manufactured by Hitachi, Ltd.) by the observation of themapping of carbon, nitrogen, and oxygen atoms.

In the filament according to the exemplary embodiment, from theviewpoint of obtaining a three-dimensional modeled article that has anexcellent bending elastic modulus and does not easily absorb water, thecontent rate of the compatibilizing agent with respect to the totalweight of the first resin, the second resin, and the compatibilizingagent is preferably 0.1% by weight or more and 10% by weight or less,more preferably 2% by weight or more and 10% by weight or less, andstill more preferably 3% by weight or more and 10% by weight or less.

In addition, in the filament according to the exemplary embodiment, thecontent rate of the compatibilizing agent with respect to the secondresin is preferably 3% by weight or more and 25% by weight or less, morepreferably 5% by weight or more and 22% by weight or less, and stillmore preferably 8% by weight or more and 22% by weight or less.

In the filament according to the exemplary embodiment, from theviewpoint of obtaining a three-dimensional modeled article that has anexcellent bending elastic modulus and does not easily absorb water, thecontent rate of the second resin with respect to the total weight of thefirst resin, the second resin, and the compatibilizing agent ispreferably 35% by weight or more and 45% by weight or less.

In the filament according to the exemplary embodiment, from theviewpoint of obtaining a three-dimensional modeled article that has anexcellent bending elastic modulus and does not easily absorb water, thecontent rate of the fiber with respect to the total weight of thefilament for three-dimensional modeling is preferably 10% by weight ormore and 65% by weight or less, more preferably 20% by weight or moreand 60% by weight or less, and still more preferably 30% by weight ormore and 60% by weight or less.

In the filament according to the exemplary embodiment, the content rateof the first resin needs to be determined in consideration of thecontent rate of the second resin, the content rate of thecompatibilizing agent, and the formability of the matrix.

The content rate of the first resin with respect to the total weight ofthe first resin, the second resin, and the compatibilizing agent ispreferably 49.9% by weight or more and 94.9% by weight or less, morepreferably 45% by weight or more and 90% by weight or less, and stillmore preferably 50% by weight or more and 70% by weight or less.

Hereinafter, the individual components of the filament according to theexemplary embodiment will be described in detail.

(First Resin and Second Resin)

The filament according to the exemplary embodiment includes resinshaving different functions such as the first resin intended to form thematrix and the second resin intended to coat the fiber.

As the first resin and the second resin each, a thermoplastic resin isused from the viewpoint of the applicability to modeling methods by FDM.

The combination of the first resin and the second resin is preferably acombination of resins having low compatibility with each other from theviewpoint of the separation of the above-described functions. Morespecifically, a combination of resins having a difference in solubilityparameter (so-called SP value) (the difference in SP value is preferably5 or more and more preferably 5 or more and 10 or less) is exemplified.

Here, the solubility parameter (SP value) refers to a value calculatedby Fedor's method. Specifically, the solubility parameter (SP value) isbased on, for example, the description of Polym. Eng. Sci., Vol. 14, p.147 (1974), and the SP value is calculated from the followingexpression.Expression: SP value=√(Ev/v)=√(ΣΔei/ΣΔvi)

(In the expression, Ev: evaporation energy (cal/mol), v: molar volume(cm³/mol), Δei: evaporation energy of each atom or atomic group, Δvi:molar volume of each atom or atomic group)

The solubility parameter (SP value) employs (cal/cm³)^(1/2) as the unit,but is expressed in a dimensionless manner without the unit according tothe convention.

The first resin and the second resin each may be formed of one kind ofresin or may be formed of two or more kinds of resins.

In the filament according to the exemplary embodiment, from theviewpoint of easily forming a three-dimensional modeled article that hasan excellent bonding elastic modulus and prevents from absorbing waterand causing deterioration, it is preferable that the first resin is apolyolefin and the second resin is a resin selected from the groupconsisting of a resin including at least one of an amide bond and animide bond, a resin including an ester bond, and a resin having abonding group including sulfur.

Depending on the kind of the compatibilizing agent (for example, a mainchain terminal-modified polyolefin), an aspect in which the first resinis a resin selected from the group consisting of a resin including atleast one of an amide bond and an imide bond, a resin including an esterbond, and a resin having a bonding group including sulfur and the secondresin is a polyolefin is also preferred.

(Polyolefin Preferred as First Resin)

The first resin is preferably a polyolefin.

One kind of polyolefin may be used singly or two or more kinds ofpolyolefins may be used in combination.

The polyolefin is a resin having a repeating unit derived from an olefinand may have a repeating unit derived from a monomer other than olefinsas long as the content of the repeating unit is 30% by weight or less ofthe entire resin.

The polyolefin is obtained by the addition polymerization of an olefin(a monomer other than olefins as necessary).

In addition, the number of the kinds of each of the olefin and themonomer other than olefins for obtaining the polyolefin may be one ormore.

The polyolefin may be a copolymer or may be a homopolymer. In addition,the polyolefin may be linear or branched.

Here, examples of the olefin include linear or branched aliphaticolefins and alicyclic olefins.

Examples of the aliphatic olefins include α-olefins such as ethylene,propylene, 1-butene, 1-hexene, 4-methyl-1-pentene, 1-octene, 1-decene,1-hexadecene, and 1-octadecene.

Examples of the alicyclic olefins include cyclopentene, cycloheptene,norbornene, 5-methyl-2-norbornene, tetracyclododecene, vinylcyclohexane,and the like.

Among these, from the viewpoint of the cost, α-olefin is preferable,ethylene and propylene are more preferable, and propylene isparticularly preferable.

In addition, as the monomer other than olefins, a well-knownaddition-polymerizable compound is selected.

Examples of the addition-polymerizable compound include styrenes such asstyrene, methyl styrene, α-methyl styrene, β-methyl styrene, t-butylstyrene, chlorostyrene, chloromethylstyrene, methoxystyrene,styrenesulfonic acid and salts thereof; (meth)acrylic acid esters suchas alkyl (meth)acrylate, benzyl (meth)acrylate, and dimethylaminoethyl(meth)acrylate; halovinyls such as vinyl chloride; vinyl esters such asvinyl acetate and vinyl propionate; vinyl ethers such as vinyl methylether; vinylidene halides such as vinylidene chloride; N-vinyl compoundssuch as N-vinylpyrrolidone; and the like.

Examples of a suitable polyolefin include polypropylene (PP),polyethylene (PE), polybutene, polyisobutylene, a coumarone-indeneresin, a terpene resin, an ethylene-vinyl acetate copolymer resin (EVA),and the like.

Among these, the polyolefin is preferably a resin having only arepeating unit derived from an olefin and, from the viewpoint of thecost, particularly preferably polypropylene.

The molecular weight of the polyolefin is not particularly limited andmay be determined depending on the kind of the resin, the modelingcondition, the use of the obtained three-dimensional modeled article,and the like.

The weight average molecular weight (Mw) of the polyolefin is, forexample, preferably from 10,000 to 300,000 and more preferably from10,000 to 200,000.

The weight average molecular weight (Mw) of the polyolefin is measuredby gel permeation chromatography (GPC) under the following conditions.

A high temperature GPC system “HLC-8321GPC/HT” is used as a GPCapparatus, and o-dichlorobenzene is used as an eluent. The polyolefin isonce melted and filtered in o-dichlorobenzene at a high temperature (atemperature of 140° C. or higher and 150° C. or lower), and the filtrateis used as a measurement sample. As the measurement conditions, thesample concentration is 0.5%, the flow rate is 0.6 ml/min, the amount ofsample injected is 10 μl, and an RI detector is used. In addition, thecalibration curve is produced from 10 samples of “polystyrene standardsample TSK standard” manufactured by Tosoh Corporation: “A-500”, “F-1”,“F-10” “F-80” “F-380”, “A-2500”, “F-4”, “F-40” “F-128”, and “F-700”.

In addition, similar to the above-described molecular weight, the glasstransition temperature (Tg) and the melting temperature (Tm) of thepolyolefin are not particularly limited and may be determined dependingon the kind of the resin, the modeling condition, the use of theobtained three-dimensional modeled article, and the like.

For example, the melting temperature (Tm) of the polyolefin ispreferably from 100° C. to 300° C. and more preferably from 150° C. to250° C.

The melting temperature (Tm) of the polyolefin is obtained by thefollowing method for measuring the melting temperature of the resin.

That is, the melting temperature (Tm, also referred to as the meltingpoint) of the resin is obtained from the “peak melting temperatureT_(pm)” described in the method for determining the melting temperaturein JIS K 7121: 1987 “Testing Methods for Transition Temperatures ofPlastics” in a DSC curve obtained by differential scanning calorimetry(DSC).

This method can also be used as the method for measuring the meltingtemperature (Tm) of the second resin, which will be described below.

The melting temperatures of the first resin and the second resin in thefilament according to the exemplary embodiment are measured by thefollowing method.

Removing the fiber from the filament, the resultant resin components arecollectively measured by DSC, so that each of the melting temperaturesof the first resin and the second resin independently appears.

In the exemplary embodiment, the melting temperatures of the first resinand the second resin may be obtained by this method.

(Resin Preferred as Second Resin)

The second resin is preferably a resin selected from the groupconsisting of a resin having at least one of an amide bond and an imidebond (hereinafter, also referred to as a specific resin a), a resinhaving an ester bond (hereinafter, also referred to as a specific resinb), and a resin having a bonding group including sulfur (hereinafter,also referred to as specific resin c).

One kind of the second resin may be used singly or two or more kinds ofthe second resins may be used in combination.

—Specific Resin a—

The specific resin a has at least one of an imide bond and an amide bondin the molecule.

The imide bond or the amide bond in the specific resin a develops anaffinity to a polar group present on the surface of the fiber (forexample, a carbon fiber). Therefore, there is a case where a part of thespecific resin a coats at least a part of the fiber surface, whereby theadhesion between the fiber and the specific resin a enhances.

Specific kinds of the specific resin a include, specifically, polyamide(PA), polyimide (PI), polyamide-imide (PAI), polyetherimide (PEI),polyamino acid, and the like.

It is preferable that the specific resin a has low compatibility withthe first resin (that is, a polyolefin) and has a different SP valuefrom the first resin (that is, a polyolefin).

Particularly, the specific resin a is preferably polyamide (PA) from theviewpoint of the capability of being molded at low temperatures, theviewpoint of further improving the bending elastic modulus, and theviewpoint of being excellent in the adhesion to the fiber.

Examples of the polyamide include a polyamide obtained by thecondensation copolymerization of dicarboxylic acid and a diamine and apolyamide obtained by the condensation of a lactam. That is, examples ofthe polyamide include polyamides having at least one of a structuralunit in which a dicarboxylic acid and a diamine arecondensation-polymerized and a structural unit in which a lactam isring-opened.

Examples of the dicarboxylic acid include oxalic acid, adipic acid,suberic acid, sebacic acid, terephthalic acid, isophthalic acid,1,4-cyclohexanedicarboxylic acid, malonic acid, succinic acid, glutaricacid, pimelic acid, azelaic acid, phthalic acid, and the like, and,among these, adipic acid and terephthalic acid are preferable.

Examples of the diamine include ethylenediamine, pentamethylenediamine,hexamethylenediamine, nonanediamine, decamethylenediamine,1,4-cyclohexanediamine, p-phenylenediamine, m-phenylenediamine,m-xylenediamine, and the like, and, among these, hexamethylenediamine ispreferable.

Examples of the lactam include ε-caprolactam, undecane lactam, lauryllactam, and the like, and, among these, ε-caprolactam is preferable.

One kind of dicarboxylic acid, diamine, or lactam described above may beused singly or two or more kinds of dicarboxylic acids, diamines, orlactams may be used in combination.

The polyamide may be an aromatic polyamide or an aliphatic polyamide.

Examples of the aromatic polyamide include MXD6 (condensation polymer ofadipic acid and meta-xylenediamine; melting point: 237° C.), Nylon 6T(condensation polymer of terephthalic acid and hexamethylenediamine;melting point: 310° C.), Nylon 9T (condensation polymer of terephthalicacid and nonanediamine; melting point: 306° C.), and the like.

Examples of the commercially available products of the aromaticpolyamide include “MXD6” manufactured by Mitsubishi Gas ChemicalCompany, Inc., “GENESTAR (registered trademark): PA6T” manufactured byKuraray Co., Ltd., “GENESTAR (registered trademark): PAST” manufacturedby Kuraray Co., Ltd. “TY-502NZ: PA6T” manufactured by Toyobo Co., Ltd.,and the like.

Examples of the aliphatic polyamide include Nylon 6 (ring-openedpolycondensate of c-caprolactam; melting point: 225° C.), Nylon 11(ring-opened polycondensate of undecane lactam; melting point: 185° C.),Nylon 12 (ring-opened polycondensate of lauryl lactam; melting point:175° C.), Nylon 66 (condensation polymer of adipic acid andhexamethylenediamine; melting point: 260° C.), Nylon 610 (condensationpolymer of sebacic acid and hexamethylenediamine; melting point: 225°C.), Nylon 612 (condensation polymer of caprolactam (having 6 carbonatoms) and lauryl lactam (having 12 carbon atoms): melting point: 220°C.), and the like.

Examples of the commercially available products of the aliphaticpolyamide include “ZYTEL (registered trademark): 7331) (PA6)”manufactured by Dupont, “ZYTEL (registered trademark): 101L (PA66)”manufactured by Dupont, and the like.

In a case where the first resin is polypropylene, among thesepolyamides, at least one kind selected from the group consisting ofMXD6, Nylon 6, and Nylon 12 may be included as the polyamide.

In addition, in a case where the first resin is polyethylene, thepolyamide may be Nylon 12, Nylon 11, or MXD6.

The molecular weight of the specific resin a is not particularly limitedand may be determined depending on which of the sea part or the islandpart the specific resin a is included, the melting temperature, or thelike. When the specific resin a is the polyamide, for example, theweight average molecular weight of the polyamide is preferably from10,000 to 300,000 and more preferably from 10,000 to 100,000.

In addition, the glass transition temperature or the melting point ofthe specific resin a may be determined depending on which of the seapart or the island part the specific resin a is included in, the meltingtemperature, or the like. When the specific resin a is the polyamide,for example, the glass transition temperature or the melting point ofthe polyamide is preferably from 100° C. to 400° C., more preferablyfrom 150° C. to 350° C., still more preferably 150° C. or higher and250° C. or lower, and most preferably 160° C. or higher and 240° C. orlower.

—Specific Resin b—

The specific resin b has an ester bond in the molecule.

The specific resin b has an ester bond, and thus the affinity to thepolar group present on the surface of the fiber (for example, a carbonfiber) is developed. Therefore, there is a case where a part of thespecific resin b coats at least a part of the fiber surface, whereby theadhesion between the fiber and the specific resin b enhances.

The specific resin b is not particularly limited as long as the specificresin b has an ester bond in the molecule.

Examples of the specific kinds of the specific resin b includethermoplastic resins having an ester bond in the main chain, andspecific examples thereof include polyesters, polycarbonates, and thelike.

As the specific resin b, a polyester is preferable.

The polyester may be any of an aliphatic polyester and an aromaticpolyester. The polyester may be, for example, a condensation-polymerizedproduct of a polyhydric alcohol and a polyhydric carboxylic acid. As thepolyester, a commercially available product may be used or a synthesizedproduct may be used.

One kind of the specific resin b may be used singly or two or more kindsof the specific resins b may be used in combination.

Examples of the polyhydric carboxylic acid include aliphaticdicarboxylic acids (for example, oxalic acid, malonic acid, maleic acid,fumaric acid, citraconic acid, itaconic acid, glutaconic acid, succinicacid, alkenylsuccinic acid, adipic acid, sebacic acid, and the like),alicyclic dicarboxylic acids (for example, cyclohexanedicarboxylic acidand the like), aromatic dicarboxylic acids (for example, terephthalicacid, isophthalic acid, phthalic acid, naphthalenedicarboxylic acid, andthe like), anhydrides thereof, and lower alkyl esters thereof (forexample, having one or more carbon atoms and five or less carbon atoms).Among these, as the polyhydric carboxylic acid, for example, thearomatic dicarboxylic acid is preferable.

As the polyhydric carboxylic acid, together with a dicarboxylic acid, atri- or higher valent carboxylic acid having a crosslinked structure ora branched structure may be used in combination. Examples of the tri- orhigher valent carboxylic acid include trimellitic acid, pyromelliticacid, anhydrides thereof, lower alkyl esters thereof (for example,having one or more carbon atoms and five or less carbon atoms), and thelike.

One kind of polyhydric carboxylic acid may be used singly or two or morekinds of polyhydric carboxylic acids may be used in combination.

Examples of the polyhydric alcohol include aliphatic diols (for example,ethylene glycol, diethylene glycol, triethylene glycol, propyleneglycol, butanediol, hexanediol, neopentyl glycol, and the like),alicyclic diols (for example, cyclohexanediol, cyclohexanedimethanol,hydrogenated bisphenol A, and the like), and aromatic diols (forexample, ethylene oxide adducts of bisphenol A, propylene oxide adductsof bisphenol A, and the like). Among these, as the polyhydric alcohol,for example, the aromatic diol and the alicyclic diol are preferable,and the aromatic diol is more preferable.

As the polyhydric alcohol, together with a diol, a tri- or higher valentpolyhydric alcohol having a crosslinked structure or a branchedstructure may be used in combination. Examples of the tri- or highervalent polyhydric alcohol include glycerin, trimethylolpropane, andpentaerythritol.

One kind of the polyhydric alcohol may be used singly or two or morekinds of the polyhydric alcohols may be used in combination.

The polyester is obtained by a well-known production method.Specifically, the polyester is obtained by, for example, a method inwhich the polymerization temperature is set to 180° C. or higher and230° C. or lower, the pressure in the reaction system is reduced asnecessary, and a reaction is caused while removing water or an alcoholgenerated during condensation.

In a case where a monomer that is the raw material is not soluble orcompatible at the reaction temperature, the monomer may be dissolved byadding a solvent having a high boiling point as a solubilizing agent. Inthis case, the polycondensation reaction is caused while distilling awaythe solubilizing agent. In a case where there is a poorly compatiblemonomer, it is preferable to condense the poorly compatible monomer andan acid or alcohol that is planned to be polycondensed with the monomerin advance and then polycondense the monomer together with a maincomponent.

Specific examples of the polyester include polyethylene terephthalate(PET), polybutylene terephthalate (PBT), and the like. Among these,polybutylene terephthalate (PBT) is preferable.

Examples of the commercially available products of the polyester include“NOVADURAN 5010R3-2” (polybutylene terephthalate) manufactured byMitsubishi Engineering-Plastics Corporation, “DURANEX 2000”(polybutylene terephthalate) manufactured by Polyplastics Co., Ltd., andthe like.

—Specific Resin c—

The specific resin c is a resin having a bonding group including sulfurin the molecule.

In the exemplary embodiment, the resin having a bonding group includingsulfur refers to a resin having a bonding group including sulfur in themain chain.

The bonding group including sulfur in the main chain develops anaffinity to the polar group present on the surface of the fiber (forexample, a carbon fiber). Therefore, there is a case where a part of thespecific resin c coats at least a part of the fiber surface, whereby theadhesion between the fiber and the specific resin c enhances.

The specific resin c is not particularly limited as long as the specificresin c has a bonding group including sulfur in the main chain.

Examples of the specific kinds of the specific resin c includethermoplastic resins linked by sulfur that is a linking group,thermoplastic resins having a sulfonyl bond in the main chain, and thelike. Specific examples thereof include polyphenylene sulfide,polysulfone, polyethersulfone, polyphenylsulfone, and the like.

The specific resin c is obtained by a well-known production method.

As the specific resin c, a commercially available product may be used ora synthesized product may be used.

One kind of the specific resin c may be used singly or two or more kindsof the specific resins c may be used in combination.

Examples of the commercially available products of the specific resin cinclude “FZ-2100” (polyphenylene sulfide) by DIC Corporation,“SUMIKAEXCEL 3600G” (polyethersulfone) by Sumitomo Chemical Co., Ltd.,and the like.

The glass transition temperatures or the melting points of the specificresin b and the specific resin c may be determined depending on which ofthe sea part or the island part the specific resin is included in, themelting temperature, or the like. The glass transition temperatures orthe melting points of the specific resin b and the specific resin c arepreferably from 100° C. to 400° C., more preferably from 150° C. to 350°C., still more preferably 150° C. or higher and 250° C. or lower, andmost preferably 160° C. or higher and 240° C. or lower.

[Fiber]

The filament according to the exemplary embodiment includes a fiber.

As the fiber, a well-known reinforcing fiber, which is applied to aresin molded article, is used, and examples thereof include a carbonfiber, a glass fiber, a metal fiber, an aramid fiber, and the like.

One kind of the fiber may be used singly or two or more kinds of thefibers may be used in combination.

Among these, the carbon fiber is preferable from the viewpoint of theexcellent affinity to the above-described second resin and thepossibility of further improving the bending elastic modulus of thethree-dimensional modeled article.

The carbon fiber has a carboxyl group on the surface. A high affinity isdeveloped between the carboxyl group and the partial structure of thesecond resin (particularly, the amide bond and/or the imide bond in thespecific resin a). Therefore, it is considered that a coating layer ofthe second resin (preferably the specific resin a) is easily formedaround the carbon fiber, and the bending elastic modulus of the moldedthree-dimensional modeled article is further improved.

As the carbon fiber, a well-known carbon fiber is used, and any of apolyacrylonitrile (PAN) carbon fibers and a pitch carbon fibers may beused.

The fiber may be a fiber that has been subjected to a well-known surfacetreatment.

When the fiber is a carbon fiber, examples of the surface treatmentinclude an oxidation treatment and a sizing treatment.

In addition, the diameter of the fiber (also referred to as the fiberdiameter), the length of the fiber (also referred to as the fiberlength), and the like are not particularly limited.

From the viewpoint of obtaining a three-dimensional modeled articlehaving a higher mechanical strength, a long fiber length is preferable,and thus a continuous fiber is more preferable as the fiber.

Here, the “continuous fiber” in the exemplary embodiment means a fiberhaving a fiber length of 10 mm or more. The fiber length of thecontinuous fiber is preferably 100 mm or more and more preferably thesame as the length of the filament according to the exemplaryembodiment.

That is, it is particularly preferable that the fiber in the filamentaccording to the exemplary embodiment is a continuous fiber that iscontinuous from the tip to the terminal of the filament.

Here, a method for measuring the fiber length is as described below.

The filament is cut along the axial direction, and the fiber length ofthe fiber in the obtained cross section is measured. Specifically, thefiber is observed with an optical microscope at a magnification of 100times, and the length of the fiber is measured. In addition, thismeasurement is carried out on 200 fibers, and the arithmetic averagevalue is regarded as the fiber length.

In addition, the fiber diameter may be appropriately determineddepending on the diameter, design mechanical characteristics, and thelike of the filament. The fiber diameter may be, for example, 5 μm ormore and 15 μm or less (preferably 5 μm or more and 10 μm or less).

Here, a method for measuring the fiber diameter is as described below.

A cross section orthogonal to the length direction of the fiber isobserved with a scanning electron microscope (SEM) at a magnification of1000 times, and the diameter of the reinforcing fiber is measured. Inaddition, this measurement is carried out on 100 reinforcing fibers, andthe average value thereof is regarded as the average diameter of thereinforcing fiber.

Furthermore, the form of the fiber is not particularly limited and maybe selected depending on a method for molding the resin molded article,the use of the resin molded article, and the like.

Examples of the form of the fiber include a single fiber, a fiber bundleincluding a number of single fibers, and the like.

As the reinforcing fiber (for example, a carbon fiber), a commerciallyavailable product may be used.

Examples of the commercially available product of the PAN carbon fiberinclude “TORAYCA (registered trademark)” by Toray Industries, Inc.,“TENAX” by Toho Tenax Co., Ltd., “PYROFIL (registered trademark)” byMitsubishi Chemical Corporation, and the like. Additionally, examples ofthe commercially available products of the PAN carbon fiber also includethe commercially available products by Hexcel Works, Inc., CytecEngineered Materials Inc., DowAksa, Formosa Plastics Corporation, andSGL Carbon Japan Co., Ltd.

Examples of the commercially available products of the pitch carbonfiber include “DIALEAD (registered trademark)” by Mitsubishi ChemicalCorporation, “GRANOC” by Nippon Graphite Fiber Co., Ltd., “KRECA” byKureha Corporation, and the like. Additionally, examples of thecommercially available products of the pitch carbon fiber also includethe commercially available products by Osaka Gas Chemicals Co., Ltd. andCytec Engineered Materials Inc.

Examples of the commercially available products of the glass fiberinclude “ROVING” by Nitto Boseki Co., Ltd. and the like.

[Compatibilizing Agent]

The compatibilizing agent is a resin that enhances the affinity betweenthe resins included in the filament (for example, the affinity betweenthe first resin and the second resin).

The compatibilizing agent may be determined depending on the resinincluded in the filament.

The compatibilizing agent is preferably a resin that has the samepartial structure as one kind of the two or more kinds of resinsincluded in the filament and has a partial structure having an affinityto another kind of resin.

In a case where the filament according to the exemplary embodimentincludes the first resin and the second resin, which are describedabove, as the two or more kinds of resins, the compatibilizing agent ispreferably a resin that has the same partial structure as the firstresin and has a partial structure having an affinity to the secondresin.

For example, as the compatibilizing agent, which is the resin that hasthe same partial structure as the first resin and has a partialstructure having an affinity to the second resin, a modified polyolefinis preferably used.

When the first resin is polypropylene (PP), the modified polyolefin ispreferably modified polypropylene (PP). Similarly, when the first resinis an ethylene-vinyl acetate copolymer resin (EVA), the modifiedpolyolefin is preferably a modified ethylene-vinyl acetate copolymerresin (EVA).

(Modified Polyolefin)

The modified polyolefin suitable as the compatibilizing agent ispreferably at least one selected from the group consisting of apolyolefin having a modified branch (hereinafter, also referred to as abranch-modified polyolefin) and a polyolefin having a modified mainchain terminal (hereinafter, also referred to as a main chainterminal-modified polyolefin).

Examples of the polyolefin having a modified branch or main chainterminal include polyolefins similar to the polyolefin that is the firstresin, and, among them, polypropylene is preferable.

Here, examples of the polypropylene include, in addition to homopolymersof propylene, random polypropylene of propylene and a small amount (forexample, 10% by weight or less in polypropylene) of a different α-olefin(for example, ethylene or the like), block polypropylene of propyleneand a different α-olefin, and the like.

—Branch-Modified Polyolefin—

The polyolefin having a modified branch refers to a polyolefin in whicha modification moiety is introduced into a side-chain.

Examples of the modification moiety that is introduced into the branchof the polyolefin include a carboxy group, a carboxylic acid anhydrideresidue, a carboxylic ester residue, an imino group, an amino group, anepoxy group, and the like.

From the viewpoint of further improving the affinity between the firstresin and the second resin (more preferably the specific resin a), themodification moiety introduced into the polyolefin preferably includes acarboxylic acid anhydride residue and particularly preferably includes amaleic anhydride residue.

As a method for producing the polyolefin having a modified branch, thereare a method in which a compound having the above-described modificationmoiety is reacted with a polyolefin and directly chemically bonded tothe polyolefin, a method in which a graft chain is formed using acompound having the above-described modification site, and this graftchain is bonded to a polyolefin, and the like.

Examples of the compound having the above-described modification moietyinclude maleic anhydride, fumaric anhydride, citric acid anhydride,N-phenyl maleimide, N-cyclohexyl maleimide, glycidyl (meth)acrylate,glycidyl vinyl benzoate, N-[4-(2,3-epoxypropoxy)-3,5-dimethylbenzyl]acrylamide, alkyl (meth)acrylate, and derivatives thereof.

Among the branch-modified polyolefins, a branch-modified polyolefinformed by reacting maleic anhydride, which is an unsaturated carboxylicacid, with a polyolefin is preferable.

Specific examples of the branch-modified polyolefin include maleicanhydride-modified polypropylene, maleic anhydride-modifiedpolyethylene, a maleic anhydride-modified ethylene-vinyl acetatecopolymer resin (EVA), and acid-modified polyolefins such as adducts orcopolymers thereof.

As the branch-modified polyolefin, a commercially available product maybe used.

Examples of the modified propylene include UMEX (registered trademark)series (100TS, 110TS, 1001, and 1010) by Sanyo Chemical Industries, Ltd.

Examples of the modified polyethylene include UMEX (registeredtrademark) series (2000) by Sanyo Chemical Industries, Ltd., MODIC(registered trademark) series by Mitsubishi Chemical Corporation, andthe like.

Examples of the modified ethylene-vinyl acetate copolymer resin (EVA)include MODIC (registered trademark) series by Mitsubishi ChemicalCorporation and the like.

In addition, as the compatibilizing agent in the case of using thespecific resin b and the specific resin c as the second resin,commercially available products below are used.

That is, “KRATON FG polymer” by Kraton Corporation, which is maleicanhydride-modified styrene-ethylene-butylene-styrene copolymer (maleicanhydride-modified SEBS), “MODIPER (registered trademark) A4300” by NOFCorporation, which is a graft polymer having a butyl acrylate-methylmethyl methacrylate copolymer (graft chain) bonded to a branch of anethylene-glycidyl methacrylate copolymer, and the like are exemplified.

—Main Chain Terminal-Modified Polyolefin—

The polyolefin having a modified main chain terminal refers to apolyolefin having a modification moiety introduced into at least one(preferably both) of the main chain terminals (namely, terminals of themain chain).

Examples of the modification moiety introduced into the main chainterminal of the polyolefin include polymers having a polar group and thelike.

Examples of the polar group in the modification moiety include acarboxyl group, metallic salts of a carboxyl group (for example, sodiumsalt, potassium salt, zinc salt, and the like), and the like.

More specifically, the main chain terminal-modified polyolefin ispreferably a block polymer in which at least one kind of polymerselected from the group consisting of poly(meth)acrylic acid and ametallic salt of poly(meth)acrylic acid is introduced into at least one(preferably both) of the main chain terminals of a polyolefin.

Here, examples of the metallic salt of poly(meth)acrylic acid include asodium salt, a potassium salt, a zinc salt, and the like ofpoly(meth)acrylic acid, and, among these, a sodium salt is preferable.

Among them, as the main chain terminal-modified polyolefin, a ternaryblock polymer of poly(meth)acrylic acid-polyolefin-poly(meth) acrylicacid and a ternary block polymer of a sodium salt of poly(meth) acrylicacid-polyolefin-a sodium salt of poly(meth)acrylic acid are preferable.

In the above-described ternary block polymers, the number averagemolecular weight of the polyolefin is preferably 1000 or more and 200000or less and more preferably 10000 or more and 50000 or less. Inaddition, in the above-described ternary block polymer, the numberaverage molecular weight of each of the poly(meth)acrylic acid or thesodium salt of poly(meth)acrylic acid is preferably 500 or more and10000 or less and more preferably 1000 or more and 5000 or less.

As the main chain terminal-modified polyolefin, a commercially availableproduct may be used.

Specific examples of the commercially available product include theternary block copolymer of polyacrylic acid-isotactic polypropylene-polyacrylic acid (Mn: 4000-23000-4000, also referred to as iPP-PAA),the ternary block copolymer of sodium polyacrylate-isotacticpolypropylene-sodium polyacrylate (Mn: 5000-23000-5000, also referred toas iPP-PAA-Na or iPP-PAA/Na), and the ternary block copolymer ofpolyacrylic acid-random polypropylene-polyacrylic acid (Mn:2500-17000-2500, also referred to as rPP-PAA) by San-ei Kogyo Corp.

—Other Components—

The resin molded article according to the exemplary embodiment mayinclude, in addition to the individual components described above, othercomponents.

Examples of the other components include well-known additives such as aflame retardant, a flame retardant promoter, an anti-sagging (drip)agent that functions when heated, a plasticizer, an antioxidant, arelease agent, a lightfast agent, a weather-proofing agent, a colorant,a pigment, a modifier, an antistatic agent, a hydrolysis inhibitor, afiller, and a reinforcing agent that is not the reinforcing fiber (talc,clay, mica, glass flakes, milled glass, glass beads, crystalline silica,alumina, silicon nitride, aluminum nitride, boron nitride, or the like).

The total amount of the other components used is, for example,preferably 10% by weight or less and more preferably 5% by weight orless with respect to the total weight of the filament according to theexemplary embodiment. The filament according to the exemplary embodimentmay not include the other components.

[Method for Producing Filament]

A method for producing the filament according to the exemplaryembodiment is not particularly limited as long as the method is capableof forming a form in which the fiber coated with the second resin isdispersed in the matrix formed of the first resin, the compatibilizingagent is interposed between the first resin and the second resin, andthe thickness of the coating layer formed of the second resin is in theabove-described range as described above.

A preferred example of the method for producing the filament accordingto the exemplary embodiment is a method in which a molten mixtureincluding the components other than the fiber (that is, the first resin,the second resin, the compatibilizing agent, and other componentsadditionally added as necessary, which is applicable below) is prepared,the fiber is impregnated with this molten mixture and then molded into alinear shape.

Particularly, at the time of preparing the molten mixture, it ispreferable to decrease the diameters of the domains of the second resindispersed in the matrix of the first resin by applying shear to themixture.

In a case where the fiber is a continuous fiber, the following method ispreferably used as the method for producing the filament according tothe exemplary embodiment.

That is, a molten mixture including the components other than the fiberis brought into contact with a continuous fiber (specifically, acontinuous fiber bundle), which is continuously fed, to impregnate thecontinuous fiber with the molten mixture, and the continuous fiberimpregnated with the molten mixture is fed to pass through a hole havinga predetermined diameter, thereby molding the fiber into a linear shape.

Even in this case, as described above, at the time of preparing themolten mixture, it is preferable to decrease the diameters of thedomains of the second resin dispersed in the matrix of the first resinby applying shear to the mixture.

<Three-Dimensional Modeled Article>

In a three-dimensional modeled article according to the exemplaryembodiment, the fiber coated with the second resin is dispersed in thematrix formed of the first resin, the compatibilizing agent isinterposed between the first resin and the second resin, the thicknessof the coating layer formed of the second resin is 0.1 μm or more and 5μm or less, and the content rate of the second resin with respect to thetotal weight of the first resin, the second resin, and thecompatibilizing agent is 30% by weight or more and 50% by weight orless, or 5% by weight or more and 15% by weight or less.

The three-dimensional modeled article according to the exemplaryembodiment is excellent in terms of the bending elastic modulus andprevents from absorbing water and causing deterioration.

Therefore, examples of the use of the three-dimensional modeled articleinclude moving bodies such as aircrafts, automobiles, bicycles, anddrones, orthotic equipment, assist suits, wearable members andapparatuses such as wearable devices, sports equipment such as soles andrackets, infrastructures such as utility poles, electric wires, andunderground tunnels, building materials, tools, a variety of cases, andthe like.

The three-dimensional modeled article according to the exemplaryembodiment is produced with the above-described filament according tothe exemplary embodiment.

More specifically, the three-dimensional modeled article according tothe exemplary embodiment is preferably produced by a method forproducing a three-dimensional modeled article according to the exemplaryembodiment, which will be described below, using the above-describedfilament according to the exemplary embodiment.

<Method and Apparatus for Producing Three-Dimensional Modeled Article>

A method for producing a three-dimensional modeled article according tothe exemplary embodiment has a step of heating the filament according tothe exemplary embodiment and a step of discharging the heated filamentfor three-dimensional modeling onto a discharge target body to form alaminate of the filament for three-dimensional modeling on the dischargetarget body.

The method for producing a three-dimensional modeled article accordingto the exemplary embodiment is carried out with a three-dimensionalmodeling apparatus according to the exemplary embodiment describedbelow.

That is, the three-dimensional modeling apparatus according to theexemplary embodiment includes a heating unit that stores the filamentfor three-dimensional modeling according to the exemplary embodiment andheats the filament for three-dimensional modeling and a discharge unitthat discharges the heated filament for three-dimensional modeling ontoa discharge target body to form a laminate of the filament forthree-dimensional modeling on the discharge target body.

The three-dimensional modeling apparatus according to the exemplaryembodiment (hereinafter, also simply referred to as the modelingapparatus) is a fusion deposition modeling (FDM)-type three-dimensionalmodeling apparatus (3D printer) and is an apparatus for modeling athree-dimensional modeled article by stacking a plurality of layersaccording to the layer data of the plurality of layers to obtain alaminate.

Hereinafter, the details of the three-dimensional modeling apparatusaccording to the exemplary embodiment will be described, and thereby themethod for producing a three-dimensional modeled article according tothe exemplary embodiment will also be described together.

An example of the three-dimensional modeling apparatus according to theexemplary embodiment will be shown below in FIG. 1, but theconfiguration of the three-dimensional modeling apparatus is not limitedthereto as long as three-dimensional modeling is possible, and some ofthe members may be omitted and separate members may be added thereto.

FIG. 1 shows a schematic view of the example of the three-dimensionalmodeling apparatus according to the exemplary embodiment.

A three-dimensional modeling apparatus 10 shown in FIG. 1 includes amodeling unit 12, a table 14, a moving mechanism 18, and a controlportion 16.

A filament 100 used in the three-dimensional modeling apparatus 10 isthe filament according to the exemplary embodiment.

(Modeling Unit 12)

As shown in FIG. 1, the modeling unit 12 includes a storing portion 20configured to store the filament 100, a feed portion 30 configured tofeed the filament 100, a heating portion (an example of a heating unit)40 configured to heat the filament 100, a discharge portion (an exampleof a discharge unit) 50 configured to discharge the filament 100, and apressure roll 60.

In the storing portion 20, the filament 100 is stored in a state ofbeing wound in a reeled shape.

The filament 100 stored in the storing portion 20 is rotated in thearrow direction and is send to a winding roll 32 in the feed portion 30.

The feed portion 30 includes the feed roll 32 and a pair of feed rolls34 and 36 and feeds the filament 100 to the heating portion 40 from thestoring portion 20.

As shown in FIG. 1, the filament 100 is wound around the winding roll 32in the feed portion 30. The filament 100 is wound around the windingroll 32 and thereby fed in a feeding direction changed downward(specifically, the direction of gravitational force) as shown in FIG. 1.

The pair of feed rolls 34 and 36 are disposed downstream of the windingroll 32 in the feeding direction of the filament 100.

The feed roll 34 is disposed on a side opposite to the feed roll 36across the filament 100, and the feed roll 34 and the feed roll 36respectively rotate in the arrow directions to sandwich and feed thefilament 100.

The pair of feed rolls 34 and 36 may have a heating portion configuredto heat the filament 100.

The heating portion 40 heats the filament 100 conveyed from the feedportion 30.

The heating portion 40 is disposed downstream of the pair of feed rolls34 and 36 in the feeding direction of the filament 100.

The heating portion 40 has a through hole through which the filament 100passes, and the filament is heated while the filament 100 passes throughthe through hole, which is heated with a heating unit (not shown)provided in the heating portion.

An example of the heating unit is a heater in which a heating wire, ahalogen lamp, or the like is used.

The heating temperature of the filament 100 depends on the kind or thelike of the filament 100 and is preferably from 100° C. to 300° C.(preferably from 180° C. to 280° C.).

The discharge portion 50 discharges the filament 100 heated by theheating portion 40 onto the table 14.

The discharge portion 50 is disposed downstream of the heating portion40 in the feeding direction of the filament 100 in a state of beingconnected to the heating portion 40.

The discharge portion 50 has a through hole continuous from the throughhole in the heating portion 40 and discharges the filament 100, whichhas passed through this through hole, to a surface 14A of the table 14from a discharge port 52.

The discharge portion 50 may have a heating unit configured to heat thethrough hole.

The pressure roll 60 pressurizes the filament 100 discharged from thedischarge portion 50.

Specifically, the pressure roll 60 presses the filament 100 against thesurface 14A of the table 14 and thereby sandwiches and pressurizes thefilament 100 with the table 14. The pressure roll 60 pressurizes thefilament 100, whereby the height of the filament 100 discharged onto thetable 14 is made uniform.

The pressure roll 60 may have a heating unit configured to heat thefilament 100.

(Table 14)

The table 14 is an example of a body onto which the filament 100 isdischarged.

The table 14 is disposed below the modeling unit 12 as shown in FIG. 1.

The table 14 has the surface 14A, which is a horizontal surface. Thefilament 100 is discharged onto the surface 14A, and a laminate of thefilament 100 is formed, thereby modeling a three-dimensional modeledarticle.

(Moving Mechanism 18)

The moving mechanism 18 is a mechanism configured to move the table 14to, for example, any position in the device vertical direction, thedevice width direction, and the device depth direction.

As the moving mechanism 18, it is possible to use, for example, atriaxial robot capable of moving the table 14 to any position in thedevice vertical direction, the device width direction, and the devicedepth direction.

(Control Portion 16)

The control portion 16 controls the individual portions of thethree-dimensional modeling apparatus 10.

Specifically, the control portion 16 has a storage portion including ROM(ROM) or a storage, in which a program is stored, and a processorconfigured to operate according to the program. The control portionreads and executes the program stored in the storage portion, therebycontrolling the operations of the individual portions of thethree-dimensional modeling apparatus 10.

The control portion 16 controls the operations of the individualportions of the three-dimensional modeling apparatus 10 based on aplurality of layer data produced from the three-dimensional data of athree-dimensional modeled article intended to be modeled such that thefollowing modeling operations are executed.

EXAMPLES

Hereinafter, the present invention will be specifically described usingexamples, but the present invention is not limited to these examples.

Examples 1 to 21 and Comparative Examples 1 to 7

A first resin, a second resin, and a compatibilizing agent according toTables 1 to 3 (the numerical values in the tables indicate amounts(unit: parts)) are kneaded with an extruder (LABTECH ENGINEERING;biaxial, ϕ: 20 mm) to obtain polymer alloy pellets.

Subsequently, a fiber according to Tables 1 to 3 (the numerical valuesin the tables indicate amounts (unit: parts)) and the above-describedpolymer alloy pellets are put into a bench for resin impregnation havinga spreading mechanism and a resin melting tank, and the carbon fiber isimpregnated with each of the components of the polymer alloy pellets,thereby producing a filament with ϕ0.6 mm.

The obtained filament is stored in a three-dimensional modelingapparatus as shown in FIG. 1, and an ISO multipurpose dumbbell testpiece is modeled under the following conditions.

The details of the three-dimensional modeling apparatus are as describedbelow.

In the three-dimensional modeling apparatus, four guide pipes tailoredfor the filament diameter are disposed as a head tip (discharge portion50). The filament is heated with an IR heater from above the guide pipes(heating portion 40) and sent to below a pressure roll (pressure roll60). A pressure is applied to the filament to form a laminate. Inaddition, the three-dimensional modeling apparatus has a mechanism foradjusting the sending rate of the filament and controls the dischargerate of the filament. The modeling unit as described above is installedon a table top-type robot (Table Top TTAC) by IAI Corporation, therebyproviding a three-dimensional modeling apparatus.

(Conditions for Modeling)

-   -   Filament heating temperature: 275° C.    -   Pressure applied to filament: 3.2 kg/cm²

The ISO multipurpose dumbbell test piece is a test piece for the ISO178bending test, and the dimensions of a measurement portion are set to 10mm in width and to 4 mm in thickness.

—Bending Elastic Modulus—

The bending elastic modulus of the obtained ISO multipurpose dumbbelltest piece is measured by a method based on ISO178 using a universaltesting device (AUTOGRAPH AG-Xplus manufactured by ShimadzuCorporation).

In addition, the obtained ISO multipurpose dumbbell test piece isimmersed in water at 80° C. for 24 hours, and then moisture on thesurface is wiped off. For the ISO multipurpose dumbbell test piece, thebending elastic modulus is measured in the same manner as describedabove.

The results are shown in Tables 1 to 3.

TABLE 1 Compar- Compar- Compar- Compar- Compar- ative ative ative ativeative Example Example Example Example Example Example Example ExampleExample Example Example 1 1 2 3 2 3 4 5 6 4 5 Components Fiber CarbonCarbon Carbon Carbon Carbon Carbon Carbon Carbon Carbon Carbon Carbon[parts by fiber fiber fiber fiber fiber fiber fiber fiber fiber fiberfiber weight] 67 67 67 67 67 67 67 67 67 67 67 First resin PP PP PP PPPP PP PP PP PP PP PP 93 91 89 81 78 78 67 53 42 40 35 Second resin PA6PA6 PA6 PA6 PA6 PA6 PA6 PA6 PA6 PA6 PA6 4 5 10 15 20 20 30 39 50 52 59Compatibilizing MAPP MAPP MAPP MAPP MAPP MAPP MAPP MAPP MAPP MAPP MAPPagent 3 4 8 4 2 2 3 8 8 8 6 Physical Coating 0.08 0.5 0.7 0.8 0.8 0.9 11 1 50 100 properties thickness of and second resin evaluation [μm]Content rate of 4 5 10 15 20 28 30 39 50 52 59 second resin [% byweight] Coating rate of 50 70 90 80 60 70 80 90 90 90 90 second resin[%] Content rate of 2 4 8 4 2 2 3 8 8 6 6 compatibilizing agent [% byweight] Bending elastic 12 15 17 15 13 14 16 26 24 24 24 modulus [GPa]Bending elastic 10 14 15 13 10 11 12 19 23 8 8 modulus after immersionin water [GPa]

TABLE 2 Comparative Comparative Example 6 Example 7 Example 8 Example 9Example 10 Example 7 Components Fiber Carbon fiber Carbon fiber Carbonfiber Carbon fiber Carbon fiber Carbon fiber [parts by weight] 67 67 6767 67 67 First resin PP PP PP PP PP PP 60.95 59 57 53 46 41 Second resinPA6 PA6 PA6 PA6 PA6 PA6 39 39 39 39 39 39 Compatibilizing agent MAPPMAPP MAPP MAPP MAPP MAPP 0.05 2 4 8 15 20 Physical properties Coatingthickness of second resin 5.5 2 1 1 0.5 0.05 and evaluation [μm] Contentrate of second resin 39 39 39 39 39 39 [% by weight] Coating rate ofsecond resin 20 70 80 90 95 95 [%] Content rate of compatibilizing agent0.05 2 4 8 15 20 [% by weight] Bending elastic modulus [GPa] 8 24 26 2930 15 Bending elastic modulus after immersion 6 14 17 23 14 10 in water[GPa]

TABLE 3 Exam- Exam- Exam- Exam- Exam- Exam- Exam- Exam- Exam- Exam-Exam- ple 11 ple 12 ple 13 ple 14 ple 15 ple 16 ple 17 ple 18 ple 19 ple20 ple 21 Components Fiber Carbon Carbon Carbon Carbon Carbon CarbonShort Glass Glass Glass Glass [parts by fiber fiber fiber fiber fiberfiber fiber fiber fiber fiber fiber weight] 67 67 67 67 67 67 67 67 6767 67 First resin PE PP PP PP PP PA6 PP PP PP PP PP 53 53 53 53 53 53 5353 53 53 53 Second resin PA6 PA66 PBT PPS PES PP PA6 PA6 PBT PPS PES 3939 39 39 39 39 39 39 39 39 39 Compatibilizing agent MAPP MAPP MAPP MAPPMAPP iPP-PAA MAPP MAPP MAPP MAPP MAPP 8 8 8 8 8 8 8 8 8 8 8 PhysicalCoating thickness of 2 2 2 3 3 2 2 3 3 4 4 properties and second resin[μm] evaluation Content rate of second 39 39 39 39 39 39 39 39 39 39 39resin [% by weight] Coating rate of second 80 90 90 90 90 90 90 90 90 9090 resin [%] Content rate of 8 8 8 8 8 8 8 8 8 8 8 compatibilizing agent[% by weight] Bending elastic modulus 25 30 28 29 30 24 18 15 15 16 17[GPa] Bending elastic modulus 24 29 26 27 28 20 17 14 14 14 15 afterimmersion in water [GPa]

The details of the individual components used in Tables 1 to 3 are asdescribed below.

—Fiber—

-   -   Carbon fiber (continuous fiber, TORAYCA (registered trademark)        T300-6000, Toray Industries, Inc.)    -   Glass fiber (continuous fiber, ROVING RS240 PG-633, Nitto Boseki        Co., Ltd.)    -   Short fiber (carbon fiber, TORAYCA (registered trademark) cut        fiber T008, Toray Industries, Inc.)

—First Resin—

-   -   PP: Polypropylene (NOVATECH (registered trademark) PP MA3, Japan        Polypropylene Corporation; melting point 165° C.)    -   PE: Polyethylene (ULTZEX 20100J, Prime Polymer Co., Ltd.;        melting point 120° C.)

—Second Resin—

-   -   PA6: Specific resin a (Nylon 6, ZYTEL (registered trademark)        7331J, Dupont; melting point 225° C.)    -   PA66: Specific resin a (Nylon 66, ZYTEL (registered trademark)        101L, Dupont; melting point 262° C.)    -   PBT: Specific resin b (polybutylene terephthalate, Mitsubishi        Engineering-Plastics Corporation; melting point 232° C.)    -   PPS: Specific resin c (polyphenylene sulfide, FZ-2100, DIC        Corporation; melting point 278° C.)    -   PES: Specific resin c (polyethersulfone, SUMIKAEXCEL, 3600        Sumitomo Chemical Co., Ltd.; melting point 288° C.)

—Compatibilizing Agent—

-   -   MAPP: Maleic anhydride-modified polypropylene (UMEX (registered        trademark) 110TS manufactured by Sanyo Chemical Industries, Ltd.    -   iPP-PAA: Ternary block copolymer of polyacrylic acid-isotactic        polypropylene-polyacrylic acid (Mn: 4000-23000-4000, San_Ei        Kougyou Ltd.)

From the above-described results, it is found that three-dimensionalmodeled articles having a high bending elastic modulus can be obtainedfrom the filaments of the examples compared with the filaments of thecomparative examples as long as the same fiber is used.

In addition, it is found that the three-dimensional modeled articlesobtained from the filaments of the examples are excellent in terms ofbending elastic modulus even after being immersed in water and are thusprevented from absorbing water and deteriorating.

The foregoing description of the exemplary embodiments of the presentinvention has been provided for the purposes of illustration anddescription. It is not intended to be exhaustive or to limit theinvention to the precise forms disclosed. Obviously, many modificationsand variations will be apparent to practitioners skilled in the art. Theembodiments were chosen and described in order to best explain theprinciples of the invention and its practical applications, therebyenabling others skilled in the art to understand the invention forvarious embodiments and with the various modifications as are suited tothe particular use contemplated. It is intended that the scope of theinvention be defined by the following claims and their equivalents.

What is claimed is:
 1. A filament for three-dimensional modeling,comprising a first resin; a second resin; a fiber; and a compatibilizingagent, wherein a fiber coated with the second resin is dispersed in amatrix formed of the first resin, the compatibilizing agent isinterposed between the first resin and the second resin, a thickness ofa coating layer formed of the second resin is 0.1 μm or more and 5 μm orless, and a content rate of the second resin with respect to a totalweight of the first resin, the second resin, and the compatibilizingagent is 30% by weight or more and 50% by weight or less, or 5% byweight or more and 15% by weight or less.
 2. The filament forthree-dimensional modeling according to claim 1, wherein a coating rateof the fiber with the second resin is 70% or more.
 3. The filament forthree-dimensional modeling according to claim 2, wherein the coatingrate of the fiber with the second resin is 80% or more.
 4. The filamentfor three-dimensional modeling according to claim 1, wherein a contentrate of the compatibilizing agent with respect to the total weight ofthe first resin, the second resin, and the compatibilizing agent is 0.1%by weight or more and 10% by weight or less.
 5. The filament forthree-dimensional modeling according to claim 2, wherein a content rateof the compatibilizing agent with respect to the total weight of thefirst resin, the second resin, and the compatibilizing agent is 0.1% byweight or more and 10% by weight or less.
 6. The filament forthree-dimensional modeling according to claim 3, wherein a content rateof the compatibilizing agent with respect to the total weight of thefirst resin, the second resin, and the compatibilizing agent is 0.1% byweight or more and 10% by weight or less.
 7. The filament forthree-dimensional modeling according to claim 4, wherein the contentrate of the compatibilizing agent with respect to the total weight ofthe first resin, the second resin, and the compatibilizing agent is 2%by weight or more and 10% by weight or less.
 8. The filament forthree-dimensional modeling according to claim 5, wherein the contentrate of the compatibilizing agent with respect to the total weight ofthe first resin, the second resin, and the compatibilizing agent is 2%by weight or more and 10% by weight or less.
 9. The filament forthree-dimensional modeling according to claim 6, wherein the contentrate of the compatibilizing agent with respect to the total weight ofthe first resin, the second resin, and the compatibilizing agent is 2%by weight or more and 10% by weight or less.
 10. The filament forthree-dimensional modeling according to claim 1, wherein the contentrate of the second resin with respect to the total weight of the firstresin, the second resin, and the compatibilizing agent is 35% by weightor more and 45% by weight or less.
 11. The filament forthree-dimensional modeling according to claim 1, wherein a content rateof the fiber with respect to a total weight of the filament forthree-dimensional modeling is 10% by weight or more and 65% by weight orless.
 12. The filament for three-dimensional modeling according to claim1, wherein the first resin is formed of a polyolefin, and the secondresin is a resin selected from the group consisting of a resin having atleast one of an amide bond and an imide bond, a resin having an esterbond, and a resin having a bonding group including sulfur.
 13. Thefilament for three-dimensional modeling according to claim 1, whereinthe compatibilizing agent is at least one kind selected from the groupconsisting of a polyolefin having a modified branched chain and apolyolefin having a modified main chain terminal.
 14. The filament forthree-dimensional modeling according to claim 1, wherein the fiber is acontinuous fiber.
 15. A three-dimensional modeled article, comprising: afirst resin; a second resin; a fiber; and a compatibilizing agent,wherein a fiber coated with the second resin is dispersed in a matrixformed of the first resin, the compatibilizing agent is interposedbetween the first resin and the second resin, a thickness of a coatinglayer formed of the second resin is 0.1 μm or more and 5 μm or less, anda content rate of the second resin with respect to a total weight of thefirst resin, the second resin, and the compatibilizing agent is 30% byweight or more and 50% by weight or less, or 5% by weight or more and15% by weight or less.
 16. A three-dimensional modeling method,comprising: heating the filament for three-dimensional modelingaccording to claim 1; and discharging the heated filament forthree-dimensional modeling onto a discharge target body to form alaminate of the filament for three-dimensional modeling.